单独一对
材料科学
三角晶系
凝聚态物理
带隙
密度泛函理论
钙钛矿(结构)
结晶学
Atom(片上系统)
电负性
化学
晶体结构
物理
计算化学
有机化学
分子
计算机科学
嵌入式系统
作者
Abhijeet J. Kale,B.B. Pal,Ambesh Dixit
标识
DOI:10.1002/pssa.202300464
摘要
Herein, density functional theory‐based comparative studies on cubic CsMX 3 ( M ‐: Pb, Sn, Ge; X‐: Cl, Br, I) and rhombohedral CsGeI 3 perovskites are reported. The structural stability indicator analysis shows that Ge‐based perovskites may exhibit small rhombohedral distortion led by lone pair (4) electrons on off‐centering Ge atom. The role of lone pair on Ge atom in rhombohedral distortion is corroborated by bond length, electronegativity, and charge density distributions. Nearly agreeable bandgap () values are noticed for cubic CsPbX 3 (X‐: Cl, Br, I) and rhombohedral CsGeI 3 , and the corresponding values are 3.04, 2.30, 1.72, and 1.45 eV, respectively. The effect of Jishi et al. reparameteried Tran–Blaha‐modified Becke–Johnson exchange‐correlation (XC) potential is discussed in context of optoelectronic properties. The changes in bandgap are attributed to the lifting of electronic degeneracy either by spin‐orbit coupling or symmetry lowering in rhombohedral distortion. The rhombohedral CsGeI 3 is thus further emphasized to account its ferroelectricity with computed total polarization () around 32.75 μC cm −2 . The suitable (1.45 eV), high absorption (≈10 5 cm −1 ), tolerable reflectivity (19%), and carrier effective masses (0.61 and 0.27) enable rhombohedral CsGeI 3 (superior 30.5% spectroscopy‐limited maximum efficiency [SLME] at 1 μm thickness) to outperform conventional CsPbI 3 (27.6% SLME at 1 μm) and others which may attract PV community to further address its underexplored promise.
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